Eosinophils infiltrate thyroids, but have no apparent role in induction or resolution of experimental autoimmune thyroiditis in interferon-γ -/- mice:

Abstract

Summary Granulomatous experimental autoimmune thyroiditis (G-EAT) is induced by mouse thyroglobulin (MTg)-sensitized splenocytes activated with MTg and interleukin (IL)-12. Our previous studies showed that, when used as donors and recipients, interferon (IFN)-γ-/- and wild-type (WT) DBA/1 mice both develop severe G-EAT. Thyroid lesions in IFN-γ-/- mice have many eosinophils and few neutrophils, while those in WT mice have extensive neutrophil infiltration and few eosinophils. Thyroid lesions in IFN-γ-/- mice consistently resolve by day 40-50, whereas those in WT mice have ongoing inflammation and fibrosis persisting for more than 60 days. To determine if the extensive infiltration of eosinophils in thyroids of IFN-γ-/- mice contributes to thyroid damage and/or early resolution of G-EAT, anti-IL-5 was used to inhibit migration of eosinophils to thyroids. G-EAT severity was compared at day 20 and day 40-50 in IFN-γ-/- recipients given anti-IL-5 or control immunoglobulin G (IgG). Thyroids of anti-IL-5-treated IFN-γ-/- mice had few eosinophils and more neutrophils at day 20, but G-EAT severity scores were comparable to those of control IgG-treated mice at both day 20 and day 40-50. Expression of chemokine (C-X-C motif) ligand 1 (CXCL1) mRNA was higher and that of chemokine (C-C motif) ligand 11 (CCL11) mRNA was lower in thyroids of anti-IL-5-treated IFN-γ-/- mice. IL-5 neutralization did not influence mRNA expression of most cytokines in IFN-γ-/- mice. Thus, inhibiting eosinophil migration to thyroids did not affect G-EAT severity or resolution in IFN-γ-/- mice, suggesting that eosinophil infiltration of thyroids occurs as a consequence of IFN-γ deficiency, but these cells have no apparent pathogenic role in G-EAT. © 2009 Blackwell Publishing Ltd.